CN113293411A - Gradient composite lead dioxide anode plate and preparation method and application thereof - Google Patents
Gradient composite lead dioxide anode plate and preparation method and application thereof Download PDFInfo
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- YADSGOSSYOOKMP-UHFFFAOYSA-N dioxolead Chemical compound O=[Pb]=O YADSGOSSYOOKMP-UHFFFAOYSA-N 0.000 title claims abstract description 112
- 239000002131 composite material Substances 0.000 title claims abstract description 98
- 238000002360 preparation method Methods 0.000 title claims abstract description 7
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical class [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 128
- 229910001220 stainless steel Inorganic materials 0.000 claims abstract description 85
- 239000010439 graphite Substances 0.000 claims abstract description 62
- 229910002804 graphite Inorganic materials 0.000 claims abstract description 62
- JKQOBWVOAYFWKG-UHFFFAOYSA-N molybdenum trioxide Chemical compound O=[Mo](=O)=O JKQOBWVOAYFWKG-UHFFFAOYSA-N 0.000 claims abstract description 61
- 239000000758 substrate Substances 0.000 claims abstract description 54
- NRTOMJZYCJJWKI-UHFFFAOYSA-N Titanium nitride Chemical compound [Ti]#N NRTOMJZYCJJWKI-UHFFFAOYSA-N 0.000 claims abstract description 28
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 claims abstract description 24
- 229910006529 α-PbO Inorganic materials 0.000 claims abstract description 19
- 230000007704 transition Effects 0.000 claims abstract description 17
- QPLDLSVMHZLSFG-UHFFFAOYSA-N Copper oxide Chemical compound [Cu]=O QPLDLSVMHZLSFG-UHFFFAOYSA-N 0.000 claims abstract description 12
- 239000005751 Copper oxide Substances 0.000 claims abstract description 12
- 229910000431 copper oxide Inorganic materials 0.000 claims abstract description 12
- 229910000476 molybdenum oxide Inorganic materials 0.000 claims abstract description 12
- 229910000480 nickel oxide Inorganic materials 0.000 claims abstract description 12
- PQQKPALAQIIWST-UHFFFAOYSA-N oxomolybdenum Chemical compound [Mo]=O PQQKPALAQIIWST-UHFFFAOYSA-N 0.000 claims abstract description 12
- GNRSAWUEBMWBQH-UHFFFAOYSA-N oxonickel Chemical compound [Ni]=O GNRSAWUEBMWBQH-UHFFFAOYSA-N 0.000 claims abstract description 12
- 239000010426 asphalt Substances 0.000 claims abstract description 11
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims abstract description 9
- 229910052802 copper Inorganic materials 0.000 claims abstract description 9
- 239000010949 copper Substances 0.000 claims abstract description 9
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 42
- 239000011159 matrix material Substances 0.000 claims description 40
- 239000002245 particle Substances 0.000 claims description 39
- 239000010935 stainless steel Substances 0.000 claims description 35
- 238000004070 electrodeposition Methods 0.000 claims description 33
- UBEWDCMIDFGDOO-UHFFFAOYSA-N cobalt(II,III) oxide Inorganic materials [O-2].[O-2].[O-2].[O-2].[Co+2].[Co+3].[Co+3] UBEWDCMIDFGDOO-UHFFFAOYSA-N 0.000 claims description 29
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 29
- 238000005406 washing Methods 0.000 claims description 27
- SQGYOTSLMSWVJD-UHFFFAOYSA-N silver(1+) nitrate Chemical compound [Ag+].[O-]N(=O)=O SQGYOTSLMSWVJD-UHFFFAOYSA-N 0.000 claims description 26
- 229910006531 α-PbO2 Inorganic materials 0.000 claims description 23
- 239000008367 deionised water Substances 0.000 claims description 20
- 229910021641 deionized water Inorganic materials 0.000 claims description 20
- 229940046892 lead acetate Drugs 0.000 claims description 20
- RLJMLMKIBZAXJO-UHFFFAOYSA-N lead nitrate Chemical compound [O-][N+](=O)O[Pb]O[N+]([O-])=O RLJMLMKIBZAXJO-UHFFFAOYSA-N 0.000 claims description 19
- 229910006654 β-PbO2 Inorganic materials 0.000 claims description 16
- 238000004140 cleaning Methods 0.000 claims description 15
- 239000011248 coating agent Substances 0.000 claims description 14
- 238000000576 coating method Methods 0.000 claims description 14
- 238000000034 method Methods 0.000 claims description 14
- 230000007935 neutral effect Effects 0.000 claims description 12
- 230000004913 activation Effects 0.000 claims description 11
- 230000002378 acidificating effect Effects 0.000 claims description 10
- 239000004332 silver Substances 0.000 claims description 10
- 238000002791 soaking Methods 0.000 claims description 10
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 claims description 9
- 230000003213 activating effect Effects 0.000 claims description 9
- 239000012153 distilled water Substances 0.000 claims description 9
- IKDUDTNKRLTJSI-UHFFFAOYSA-N hydrazine monohydrate Substances O.NN IKDUDTNKRLTJSI-UHFFFAOYSA-N 0.000 claims description 9
- 229910017604 nitric acid Inorganic materials 0.000 claims description 9
- 229910052709 silver Inorganic materials 0.000 claims description 9
- 229910001961 silver nitrate Inorganic materials 0.000 claims description 7
- CDBYLPFSWZWCQE-UHFFFAOYSA-L sodium carbonate Substances [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 claims description 7
- 229910000029 sodium carbonate Inorganic materials 0.000 claims description 7
- 238000006243 chemical reaction Methods 0.000 claims description 6
- NWZSZGALRFJKBT-KNIFDHDWSA-N (2s)-2,6-diaminohexanoic acid;(2s)-2-hydroxybutanedioic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O.NCCCC[C@H](N)C(O)=O NWZSZGALRFJKBT-KNIFDHDWSA-N 0.000 claims description 5
- 101710134784 Agnoprotein Proteins 0.000 claims description 5
- 239000002253 acid Substances 0.000 claims description 5
- 239000002105 nanoparticle Substances 0.000 claims description 5
- 239000011148 porous material Substances 0.000 claims description 5
- 239000004575 stone Substances 0.000 claims 1
- 229910000978 Pb alloy Inorganic materials 0.000 abstract description 7
- 230000002035 prolonged effect Effects 0.000 abstract description 7
- 229910052751 metal Inorganic materials 0.000 abstract description 6
- 239000002184 metal Substances 0.000 abstract description 6
- 239000000463 material Substances 0.000 abstract description 5
- 238000009854 hydrometallurgy Methods 0.000 abstract description 2
- 230000007797 corrosion Effects 0.000 description 9
- 238000005260 corrosion Methods 0.000 description 9
- 238000005868 electrolysis reaction Methods 0.000 description 7
- 239000003792 electrolyte Substances 0.000 description 7
- 239000000126 substance Substances 0.000 description 5
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 4
- 238000007747 plating Methods 0.000 description 4
- 229910010271 silicon carbide Inorganic materials 0.000 description 4
- PUZPDOWCWNUUKD-UHFFFAOYSA-M sodium fluoride Chemical compound [F-].[Na+] PUZPDOWCWNUUKD-UHFFFAOYSA-M 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- JPVYNHNXODAKFH-UHFFFAOYSA-N Cu2+ Chemical compound [Cu+2] JPVYNHNXODAKFH-UHFFFAOYSA-N 0.000 description 3
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 3
- 229910045601 alloy Inorganic materials 0.000 description 3
- 239000000956 alloy Substances 0.000 description 3
- 239000011575 calcium Substances 0.000 description 3
- 229910052791 calcium Inorganic materials 0.000 description 3
- 229910001431 copper ion Inorganic materials 0.000 description 3
- 238000000151 deposition Methods 0.000 description 3
- 230000008021 deposition Effects 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 150000002739 metals Chemical class 0.000 description 3
- 239000010936 titanium Substances 0.000 description 3
- 229910052719 titanium Inorganic materials 0.000 description 3
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
- 238000007605 air drying Methods 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000005265 energy consumption Methods 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 230000010287 polarization Effects 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000011775 sodium fluoride Substances 0.000 description 2
- 235000013024 sodium fluoride Nutrition 0.000 description 2
- 239000010963 304 stainless steel Substances 0.000 description 1
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 description 1
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 1
- 229910000589 SAE 304 stainless steel Inorganic materials 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- 239000010406 cathode material Substances 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 239000011572 manganese Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- ZNNZYHKDIALBAK-UHFFFAOYSA-M potassium thiocyanate Chemical compound [K+].[S-]C#N ZNNZYHKDIALBAK-UHFFFAOYSA-M 0.000 description 1
- 229940116357 potassium thiocyanate Drugs 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 239000002987 primer (paints) Substances 0.000 description 1
- 238000004080 punching Methods 0.000 description 1
- 238000007788 roughening Methods 0.000 description 1
- 239000002893 slag Substances 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
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- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25C—PROCESSES FOR THE ELECTROLYTIC PRODUCTION, RECOVERY OR REFINING OF METALS; APPARATUS THEREFOR
- C25C7/00—Constructional parts, or assemblies thereof, of cells; Servicing or operating of cells
- C25C7/02—Electrodes; Connections thereof
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- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25C—PROCESSES FOR THE ELECTROLYTIC PRODUCTION, RECOVERY OR REFINING OF METALS; APPARATUS THEREFOR
- C25C1/00—Electrolytic production, recovery or refining of metals by electrolysis of solutions
- C25C1/12—Electrolytic production, recovery or refining of metals by electrolysis of solutions of copper
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25D—PROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
- C25D9/00—Electrolytic coating other than with metals
- C25D9/04—Electrolytic coating other than with metals with inorganic materials
- C25D9/06—Electrolytic coating other than with metals with inorganic materials by anodic processes
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P10/00—Technologies related to metal processing
- Y02P10/20—Recycling
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- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Electrodes For Compound Or Non-Metal Manufacture (AREA)
Abstract
The invention relates to a gradient composite lead dioxide anode plate and a preparation method and application thereof, belonging to the technical field of hydrometallurgy anode plates. The gradient composite lead dioxide anode plate comprises an activated graphite substrate, a stainless steel wire mesh transition layer, a composite alpha-PbO 2 intermediate layer and a composite beta-PbO 2 active layer from inside to outside in sequence, wherein the graphite substrate comprises scaly graphite powder, modified asphalt, copper oxide, ferrous oxide, nickel oxide and molybdenum oxide, the composite alpha-PbO 2 intermediate layer is alpha-PbO 2-nano titanium nitride, and the composite beta-PbO 2 active layer is silver-doped beta-PbO 2-nano molybdenum trioxide. The gradient composite lead dioxide anode plate has good conductivity, and compared with the traditional lead alloy, the gradient composite lead dioxide anode plate has the advantages that the material cost is low, anode mud cannot be generated when the gradient composite lead dioxide anode plate is used under high current density, the service life is prolonged by more than 2 times, the cell voltage can be reduced by 300mV, and the current efficiency is improved by 3-6% in extracting metal copper.
Description
Technical Field
The invention relates to a gradient composite lead dioxide anode plate and a preparation method and application thereof, belonging to the technical field of hydrometallurgy anode plates.
Background
Currently, anodes used for hydrometallurgical electrolysis of metals are lead alloy anodes and graphite anodes or titanium-based anodes. But the lead alloy anode has the main defects of serious corrosion, poor conductivity, high power consumption and serious lead pollution of products; the graphite anode has high power consumption, large brittleness and large loss and cannot be used under high current density; the titanium-based anode is mainly high in price and poor in conductivity. Particularly, the lead alloy anode is adopted under the condition that the copper price gradually rises recently, and the anode under the condition of high current density has high power consumption and very large lead alloy consumption.
Early stage PbO2The electrode is directly formed by anode oxidation of lead, but the electrode has poor mechanical strength and is not suitable for industrial application.
The prior inert lead dioxide anode selects titanium or graphite as a substrate material, and is subjected to surface roughening treatment, bottom coating and alpha-PbO coating2Intermediate layer and electroplated beta-PbO2Plating to obtain PbO by the basic process2And an electrode. The advantage is that (1) it can be operated at high current densities; (2) can inhibit the generation of mud; (3) the oxidation efficiency can be improved; (4) good corrosion resistance and long service life; (5) in the electrodeposition of nonferrous metals, no chemical conversion treatment is needed, the amount of lead mixed into cathode products is reduced, the corrosion resistance to chlorine is good, chlorine can be removed, manganese slag is not generated, and the current efficiency for extracting nonferrous metals is high. But PbO produced by such plating2The electrode is used as an insoluble anode, and the following problems can occur in use: (1) basic graphiteSwelling easily in solution and poor corrosion resistance, (2) PbO2The combination of the deposition layer and the surface of the electrode is not tight or the deposition layer is not uniform; (3) poor conductivity of the primer coating, and alpha-PbO2The middle layer has poor bonding and is easy to generate large voltage drop; (4) PbO2The interface resistance of the deposition layer and the matrix is large, the heat generated in the electrolytic process is serious and easy to peel off or corrode, and the service life is short; (5) low current efficiency although PbO2The electrocatalytic activity of the electrode is high, but the current efficiency in non-ferrous metal electrodeposition applications is not very high.
Disclosure of Invention
The invention provides a gradient composite lead dioxide anode plate and a preparation method and application thereof aiming at the problems of the inert lead dioxide anode in the prior art, the gradient composite lead dioxide anode plate has good electrode conductivity, low cell voltage in the electrolytic process, long service life and low energy consumption, and compared with the traditional lead alloy, the material cost is low, anode mud cannot be generated when the anode plate is used under high current density, the service life is prolonged by more than 2 times, the cell voltage can be reduced by 300mV, and the current efficiency is improved by 3-6%; the gradient composite lead dioxide anode has good performance and strong corrosion resistance in alkaline electrodeposition copper liquid; the corrosion resistance and other performances in the acidic electro-deposited copper liquid are also relatively excellent.
The gradient composite lead dioxide anode plate sequentially comprises an activated graphite substrate, a stainless steel wire mesh transition layer and a composite alpha-PbO from inside to outside2Intermediate layer and composite beta-PbO2The graphite substrate comprises flaky graphite powder, modified asphalt, copper oxide, ferrous oxide, nickel oxide and molybdenum oxide, and is compounded with alpha-PbO2The intermediate layer is alpha-PbO2-nano titanium nitride, composite beta-PbO2The active layer is silver-doped beta-PbO2-nano molybdenum trioxide;
the graphite substrate comprises, by mass, 100% of a graphite substrate, 10-18% of modified asphalt, 0.01-0.2% of copper oxide, 0.01-0.1% of ferrous oxide, 0.01-0.05% of nickel oxide, 0.01-0.05% of molybdenum oxide and the balance of flaky graphite powder;
the surface of the graphite substrate contains Ag-Co3O4Active layer of Co3O4Is nanoparticle with particle size of 10-100nm, and Ag-Co3O4The mass content of Ag in the activation layer is 20-50%;
further, the graphite substrate has a thickness of 12 mm-25 mm, a length of 300 mm-1000 mm and a width of 200 mm-600 mm; a plurality of through holes are uniformly formed in the graphite substrate, the through holes are round holes or elliptical holes, the diameter of each round hole is 15-25 mm, the long diameter of each elliptical hole is 20-40 mm, and the short diameter of each elliptical hole is 10-25 mm;
the meshes of the stainless steel mesh transition layer are 80-800 meshes, the wire diameter is 0.02-2 mm, the stainless steel is 316L or 304 stainless steel, and 800 meshes of carborundum are sprayed on the surface of the stainless steel mesh transition layer;
the alpha-PbO2-the thickness of the nano titanium nitride is 0.05-0.5 mm, the content of titanium nitride particles is 0.1-5 wt.%, and the particle size of the nano titanium nitride is 20-60 nm;
the silver-doped beta-PbO2-the thickness of the nano molybdenum trioxide is 0.1-1.5 mm, the content of molybdenum trioxide particles is 0.1-0.5 wt.%, the particle size of the nano molybdenum trioxide is 80-200nm, and the content of silver is 0.01-0.15 wt.%.
The gradient composite lead dioxide anode plate is characterized in that a graphite plate is subjected to activation treatment to obtain an activated graphite matrix, the surface of the activated graphite matrix is coated with a stainless steel screen bottom layer to obtain an activated graphite matrix/stainless steel screen bottom layer, and the surface of the activated graphite matrix/stainless steel screen bottom layer is subjected to electrodeposition to prepare composite alpha-PbO2The middle layer is used for obtaining the activated graphite matrix/stainless steel wire mesh bottom layer/composite alpha-PbO2Middle layer, activated graphite matrix/stainless steel wire net bottom layer/composite alpha-PbO2Surface electrodeposition of intermediate layer composite beta-PbO2The active layer obtains a gradient composite lead dioxide anode plate.
The preparation method of the gradient composite lead dioxide anode plate comprises the following specific steps:
(1) placing a graphite plate in NaOH solution, soaking for 0.5-1 h at the temperature of 60-80 ℃, cleaning with distilled water until the cleaning solution is neutral, and then placing in HNO3Soaking in the solution for 10-20 min, cleaning with distilled water until the cleaning solution is neutral, and airing to obtain a pretreated graphite plate;
(2) placing the graphite plate pretreated in the step (1) in the solution A, stirring and reacting for 2-20 min at the pH value of 9-11 and the temperature of 40-80 ℃, and washing with deionized water to obtain the solution containing Ag-Co3O4An activated graphite matrix of the activation layer; wherein solution A contains AgNO3、Na2CO3Hydrazine hydrate and nano Co3O4;
(3) Coating the surface of the activated graphite substrate in the step (2) with a stainless steel wire mesh transition layer, then placing the activated graphite substrate in HC1 solution for reaction for 0.5-2 min, and washing with deionized water until the washing solution is neutral to obtain an activated graphite substrate/stainless steel wire mesh bottom layer;
(4) placing the activated graphite substrate/stainless steel wire mesh bottom layer obtained in the step (3) in an alkaline lead acetate solution, performing electrodeposition for 1-3 h at the temperature of 40-60 ℃ by taking a stainless steel plate as a cathode, and washing with deionized water to obtain the activated graphite substrate/stainless steel wire mesh bottom layer/composite alpha-PbO2An intermediate layer; wherein the alkaline lead acetate solution contains lead acetate, NaOH and nano titanium nitride particles;
(5) activating the graphite substrate/stainless steel wire mesh bottom layer/composite alpha-PbO in the step (4)2The middle layer is placed in an acidic lead nitrate solution, a stainless steel pore plate is used as a cathode, electrodeposition is carried out for 2-8 hours at the temperature of 40-80 ℃, and deionized water is adopted for washing to obtain a gradient composite lead dioxide anode plate; wherein the acid lead nitrate solution contains lead nitrate and HNO3Nano molybdenum trioxide particles and silver nitrate;
the concentration of the NaOH solution in the step (1) is 20-40 wt.%, and HNO is added3The concentration of the solution is 10-20 wt.%;
AgNO in the solution A in the step (2)3The concentration is 1-3 g/L, Na2CO3The concentration is 5-20 g/L, the concentration of hydrazine hydrate is 2-20 mL/L, and the concentration of nano Co is3O4The concentration is 0.2-3 g/L;
the HC1 solution concentration in the step (3) is 5-10 wt.%;
the concentration of lead acetate in the alkaline lead acetate solution in the step (4) is 40-80 g/L, the concentration of NaOH is 140-200 g/L, the concentration of nano titanium nitride particles is 2-10 g/L, and the current density of an anode for electrodeposition is 0.2-2A/dm2;
The concentration of lead nitrate in the acidic lead nitrate solution in the step (5) is 100-300 g/L, HNO3The concentration is 20-50 g/L, the concentration of the nano molybdenum trioxide particles is 10-30 g/L, the concentration of silver nitrate is 20-50 g/L, and the current density of an anode of electrodeposition is 1-6A/dm2;
The gradient composite lead dioxide anode plate is used as an anode plate in copper electrodeposition.
The invention has the beneficial effects that:
(1) according to the invention, the graphite matrix is doped with a small amount of copper oxide, ferrous oxide, nickel oxide, molybdenum oxide and other substances, so that the corrosion resistance of the matrix can be improved, the punching treatment is performed, the firmness of lead dioxide and the matrix is improved, the mobility of electrolyte in an electrolytic bath is increased, the concentration polarization of the solution is reduced, and the current efficiency of a cathode product is improved;
(2) the graphite surface of the invention is Ag-Co3O4The activation layer greatly improves the electrical conductivity of the anode, and leads the graphite and the alpha-PbO with poor electrical conductivity2The layer does not generate interface resistance;
(3) the stainless steel wire mesh is coated on the surface of the graphite, so that the strength of the graphite is increased, the internal stress of a lead dioxide coating is reduced, the conduction efficiency of a polar plate is obviously improved, and the subsequently deposited alpha-PbO is enabled to be2The binding force is firm, and the service life of the anode is greatly prolonged; composite electro-deposited alpha-PbO2The plating solution is deposited in a lead acetate system, the dissolved lead salt is more, the concentration of the main salt is high, the concentration polarization of lead ions in the solution is reduced, and red Pb is avoided3O4The production of a substance;
(4) the nano TiN has the structural material with high melting point, high hardness, good chemical stability and small wetting with metal, has higher conductivity and superconductivity, and is prepared in alpha-PbO2The hardness, conductivity and chemical stability of the plating layer can be improved;
(5) the invention introduces beta-PbO into the nano molybdenum trioxide and the conductive silver2Avoids the generation of coating cracks in the coating, greatly improves the conductivity and corrosion resistance of the composite coating, and improves the precipitation of the anodeOxygen electrocatalytic activity;
(6) the gradient composite lead dioxide anode plate electrode has good conductivity, low tank voltage in the electrolytic process, long service life and low energy consumption, and compared with the traditional lead alloy, the gradient composite lead dioxide anode plate electrode has the advantages of low material cost, no anode mud generated by using the gradient composite lead dioxide anode plate electrode under high current density, long service life prolonged by more than 2 times, tank voltage reduced by 300mV and current efficiency improved by 3-6 percent; in the using process, the high-grade cathode material has good corrosion resistance, and can be prepared into high-grade cathode products.
Drawings
FIG. 1 is a schematic structural view of a gradient composite lead dioxide anode;
in the figure: 1-graphite matrix, 2-stainless steel wire mesh and 3-composite alpha-PbO2Intermediate layer, 4-complex beta-PbO2And an active layer.
Detailed Description
The present invention will be described in further detail with reference to specific embodiments, but the scope of the present invention is not limited to the description.
Example 1: the gradient composite lead dioxide anode plate (see fig. 1) of the embodiment sequentially comprises an activated graphite substrate 1, a stainless steel wire mesh transition layer 2 and a composite alpha-PbO from inside to outside2 Intermediate layer 3 and composite beta-PbO2The active layer 4, the graphite substrate comprises scaly graphite powder, modified asphalt, copper oxide, ferrous oxide, nickel oxide and molybdenum oxide, and is compounded with alpha-PbO2The intermediate layer is alpha-PbO2-nano titanium nitride, composite beta-PbO2The active layer is silver-doped beta-PbO2-nano molybdenum trioxide;
the graphite base comprises, by mass, 100% of a graphite base body, 10% of modified asphalt, 0.01% of copper oxide, 0.01% of ferrous oxide, 0.01% of nickel oxide, 0.01% of molybdenum oxide and the balance of flaky graphite powder; the graphite substrate has the thickness of 12mm, the length of 300mm and the width of 200 mm; a plurality of through holes are uniformly formed in the graphite substrate, the through holes are round holes, and the diameter of each round hole is 15 mm; the surface of the graphite substrate contains Ag-Co3O4Active layer of Co3O4Is nano-particle with particle size of 10nm, Ag-Co3O4The mass content of Ag in the activation layer is 20%,Co3O4The mass content of (A) is 80%;
the mesh of the stainless steel mesh transition layer is 80 meshes, the diameter of the wire is 0.02mm, the stainless steel is 316L, and 800 meshes of carborundum are sprayed on the surface;
α-PbO2-the thickness of the nano titanium nitride is 0.05mm, the content of titanium nitride particles is 0.1 wt.%, and the particle size of the nano titanium nitride is 20 nm;
silver doped beta-PbO2-the thickness of the nano molybdenum trioxide is 0.1mm, the content of molybdenum trioxide particles is 0.1 wt.%, the particle size of the nano molybdenum trioxide is 80nm, the silver content is 0.01 wt.%;
the method comprises the steps of preparing a gradient composite lead dioxide anode plate, activating a graphite plate to obtain an activated graphite matrix, coating the surface of the activated graphite matrix with a stainless steel screen bottom layer to obtain an activated graphite matrix/stainless steel screen bottom layer, and preparing composite alpha-PbO on the surface of the activated graphite matrix/stainless steel screen bottom layer through electrodeposition2The middle layer is used for obtaining the activated graphite matrix/stainless steel wire mesh bottom layer/composite alpha-PbO2Middle layer, activated graphite matrix/stainless steel wire net bottom layer/composite alpha-PbO2Surface electrodeposition of intermediate layer composite beta-PbO2The active layer obtains a gradient composite lead dioxide anode plate, and the method comprises the following specific steps:
(1) placing graphite plate in NaOH solution with concentration of 20 wt.%, soaking at 60 deg.C for 0.5h, cleaning with distilled water until the cleaning solution is neutral, and placing in HNO with concentration of 10 wt.%3Soaking in the solution for 10min, washing with distilled water until the washing solution is neutral, and air drying to obtain a pretreated graphite plate;
(2) placing the graphite plate pretreated in the step (1) in the solution A, stirring and reacting for 5min at the temperature of 40 ℃ and the pH value of 9, washing with deionized water to obtain the solution containing Ag-Co3O4An activated graphite matrix of the activation layer; wherein the solution A contains 1g/L AgNO35g/L of Na2CO32mL/L hydrazine hydrate and 0.2g/L nano Co3O4;
(3) Coating a stainless steel wire mesh transition layer on the surface of the activated graphite substrate in the step (2), fixing the stainless steel wire mesh by using a stainless steel rivet, then placing the stainless steel wire mesh in an HC1 solution with the concentration of 5 wt.% for reaction for 0.5min, and washing the stainless steel wire mesh with deionized water to obtain an activated graphite substrate/stainless steel wire mesh bottom layer;
(4) placing the activated graphite substrate/stainless steel wire mesh bottom layer obtained in the step (3) in an alkaline lead acetate solution, performing electrodeposition for 1h at the temperature of 40 ℃ by taking a stainless steel plate as a cathode, and washing by using deionized water to obtain the activated graphite substrate/stainless steel wire mesh bottom layer/composite alpha-PbO2An intermediate layer; wherein the alkaline lead acetate solution contains lead acetate (Pb (CH)3COO)2)40g/L, NaOH 140g/L and 2g/L of nano titanium nitride particles, and the anode current density of the electrodeposition is 0.2A/dm2;
(5) Activating the graphite substrate/stainless steel wire mesh bottom layer/composite alpha-PbO in the step (4)2The intermediate layer is placed in an acidic lead nitrate solution, a stainless steel pore plate is used as a cathode, electrodeposition is carried out for 2 hours at the temperature of 40 ℃, and deionized water is adopted for washing to obtain a gradient composite lead dioxide anode plate; wherein the acidic lead nitrate solution contains lead nitrate (Pb (NO)3)2)100g/L、HNO320g/L nano molybdenum trioxide (MoO)3) Particles 10g/L and silver nitrate (AgNO)3)20g/L, the anode current density of the electrodeposition is 1A/dm2;
In the present embodiment, the gradient composite lead dioxide anode plate is in the alkaline copper electrolyte, and the electrolysis conditions are as follows: the concentration of copper ions in the electrolyte is 5g/L, the concentration of sulfate ions is 120g/L, the concentration of potassium thiocyanate is 1g/L, the concentration of calcium hydroxide is 1g/L, the concentration of sodium hydroxide is 8g/L, and the current density is 200A/dm2The electrolysis temperature is 25 ℃, the electrical efficiency of the gradient composite lead dioxide anode is improved by 2.0 percent compared with the traditional lead-calcium (0.06 percent) tin (1.0 percent) alloy anode plate, the cell voltage is low by 180mV, and the service life is prolonged by 1.6 times.
Example 2: the gradient composite lead dioxide anode plate (see fig. 1) of the embodiment sequentially comprises an activated graphite substrate 1, a stainless steel wire mesh transition layer 2 and a composite alpha-PbO from inside to outside2 Intermediate layer 3 and composite beta-PbO2The active layer 4, the graphite substrate comprises scaly graphite powder, modified asphalt, copper oxide, ferrous oxide, nickel oxide and molybdenum oxide, and is compounded with alpha-PbO2The intermediate layer is alpha-PbO2-nano titanium nitride, composite beta-PbO2The active layer is silver-doped beta-PbO2-nano molybdenum trioxide;
the graphite matrix comprises, by mass, 100% of modified asphalt, 0.1% of copper oxide, 0.05% of ferrous oxide, 0.03% of nickel oxide, 0.03% of molybdenum oxide and the balance of flaky graphite powder; the graphite substrate has the thickness of 12mm, the length of 300mm and the width of 200 mm; a plurality of through holes are uniformly formed in the graphite substrate, the through holes are elliptical holes, and the major diameter of each elliptical hole is 30mm and the minor diameter of each elliptical hole is 15 mm; the surface of the graphite substrate contains Ag-Co3O4Active layer of Co3O4Is nano-particle with particle size of 30nm, Ag-Co3O4The mass content of Ag in the active layer is 50 percent, and Co3O4The mass content of (A) is 50%;
the mesh of the stainless steel mesh transition layer is 400 meshes, the diameter of the wire is 1mm, the stainless steel is 316L, and 800 meshes of carborundum are sprayed on the surface;
α-PbO2-the thickness of the nano titanium nitride is 0.2mm, the content of titanium nitride particles is 1 wt.%, and the particle size of the nano titanium nitride is 30 nm;
silver doped beta-PbO2-thickness of nano molybdenum trioxide is 0.4mm, content of molybdenum trioxide particles is 0.3 wt.%, particle size of nano molybdenum trioxide is 120nm, silver content is 0.1 wt.%;
the method comprises the steps of preparing a gradient composite lead dioxide anode plate, activating a graphite plate to obtain an activated graphite matrix, coating the surface of the activated graphite matrix with a stainless steel screen bottom layer to obtain an activated graphite matrix/stainless steel screen bottom layer, and preparing composite alpha-PbO on the surface of the activated graphite matrix/stainless steel screen bottom layer through electrodeposition2The middle layer is used for obtaining the activated graphite matrix/stainless steel wire mesh bottom layer/composite alpha-PbO2Middle layer, activated graphite matrix/stainless steel wire net bottom layer/composite alpha-PbO2Surface electrodeposition of intermediate layer composite beta-PbO2The active layer obtains a gradient composite lead dioxide anode plate, and the method comprises the following specific steps:
(1) placing graphite plate in NaOH solution with concentration of 30 wt.%, soaking at 70 deg.C for 1h, cleaning with distilled water until the cleaning solution is neutral, and placing in HNO with concentration of 15 wt.%3Soaking in the solution for 15min, and cleaning with distilled waterThe washing liquid is neutral, and the pretreated graphite plate is obtained by airing;
(2) placing the graphite plate pretreated in the step (1) in the solution A, stirring and reacting for 8min at the temperature of 60 ℃ and the pH value of 10, and washing with deionized water to obtain the graphite plate containing Ag-Co3O4An activated graphite matrix of the activation layer; wherein the solution A contains 2g/L AgNO315g/L of Na2CO310mL/L hydrazine hydrate and 0.2g/L nano Co3O4;
(3) Coating a stainless steel wire mesh transition layer on the surface of the activated graphite substrate in the step (2), fixing the stainless steel wire mesh by using a stainless steel rivet, then placing the stainless steel wire mesh in an HC1 solution with the concentration of 10 wt.% for reaction for 1min, and washing the stainless steel wire mesh with deionized water to obtain an activated graphite substrate/stainless steel wire mesh bottom layer;
(4) placing the activated graphite substrate/stainless steel wire mesh bottom layer obtained in the step (3) in an alkaline lead acetate solution, performing electrodeposition for 1h at the temperature of 40 ℃ by taking a stainless steel plate as a cathode, and washing by using deionized water to obtain the activated graphite substrate/stainless steel wire mesh bottom layer/composite alpha-PbO2An intermediate layer; wherein the alkaline lead acetate solution contains lead acetate (Pb (CH)3COO)2)50g/L, NaOH 140g/L and 3g/L of nano titanium nitride particles, and the anode current density of electrodeposition is 0.5A/dm2;
(5) Activating the graphite substrate/stainless steel wire mesh bottom layer/composite alpha-PbO in the step (4)2The intermediate layer is placed in an acidic lead nitrate solution, a stainless steel pore plate is used as a cathode, electrodeposition is carried out for 3 hours at the temperature of 70 ℃, and deionized water is adopted for washing to obtain a gradient composite lead dioxide anode plate; wherein the acidic lead nitrate solution contains lead nitrate (Pb (NO)3)2)300g/L、HNO340g/L nano molybdenum trioxide (MoO)3) Particles 20g/L and silver nitrate (AgNO)3)30g/L, the anode current density of the electrodeposition is 3A/dm2;
In the acid copper electrolyte, the gradient composite lead dioxide anode plate of the embodiment has the following electrolysis conditions: the concentration of copper ions in the electrolyte is 45g/L, the concentration of sulfuric acid is 180g/L, 50mg/L of sodium fluoride and 800mg/L C1-ions are adopted, the electrolysis temperature is 60 ℃, and the current density is 400A/dm2The gradient composite lead dioxide anodeThe efficiency is improved by 6 percent compared with the traditional lead-calcium (0.06 percent) tin (1.0 percent) alloy anode plate, the tank voltage is reduced by 300mV, and the service life is prolonged by 3 times.
Example 3: the gradient composite lead dioxide anode plate (see fig. 1) of the embodiment sequentially comprises an activated graphite substrate 1, a stainless steel wire mesh transition layer 2 and a composite alpha-PbO from inside to outside2 Intermediate layer 3 and composite beta-PbO2The active layer 4, the graphite substrate comprises scaly graphite powder, modified asphalt, copper oxide, ferrous oxide, nickel oxide and molybdenum oxide, and is compounded with alpha-PbO2The intermediate layer is alpha-PbO2-nano titanium nitride, composite beta-PbO2The active layer is silver-doped beta-PbO2-nano molybdenum trioxide;
based on the mass of the graphite matrix as 100%, the graphite matrix contains 18% of modified asphalt, 0.2% of copper oxide, 0.1% of ferrous oxide, 0.05% of nickel oxide, 0.05% of molybdenum oxide and the balance of flaky graphite powder; the thickness of the graphite substrate is 15mm, the length is 1000mm, and the width is 600 mm; a plurality of through holes are uniformly formed in the graphite substrate, the through holes are round holes, and the diameter of each round hole is 25 mm; the surface of the graphite substrate contains Ag-Co3O4Active layer of Co3O4Is nano-particle with particle size of 100nm, Ag-Co3O4The mass content of Ag in the activation layer is 30 percent, and Co3O4The mass content of (A) is 70%;
the mesh of the stainless steel mesh transition layer is 800 meshes, the diameter of the wire is 2mm, the stainless steel is 304, and 800 meshes of carborundum are sprayed on the surface of the stainless steel mesh transition layer;
α-PbO2-the thickness of the nano titanium nitride is 0.5mm, the content of titanium nitride particles is 5 wt.%, and the particle size of the nano titanium nitride is 60 nm;
silver doped beta-PbO2-thickness of nano molybdenum trioxide is 1.5mm, content of molybdenum trioxide particles is 0.5 wt.%, particle size of nano molybdenum trioxide is 200nm, silver content is 0.15 wt.%;
the method comprises the steps of preparing a gradient composite lead dioxide anode plate, activating a graphite plate to obtain an activated graphite matrix, coating the surface of the activated graphite matrix with a stainless steel screen bottom layer to obtain an activated graphite matrix/stainless steel screen bottom layer, and preparing composite alpha-PbO on the surface of the activated graphite matrix/stainless steel screen bottom layer through electrodeposition2The middle layer is used for obtaining the activated graphite matrix/stainless steel wire mesh bottom layer/composite alpha-PbO2Middle layer, activated graphite matrix/stainless steel wire net bottom layer/composite alpha-PbO2Surface electrodeposition of intermediate layer composite beta-PbO2The active layer obtains a gradient composite lead dioxide anode plate, and the method comprises the following specific steps:
(1) placing graphite plate in NaOH solution with concentration of 40 wt.%, soaking at 80 deg.C for 1h, cleaning with distilled water until the cleaning solution is neutral, and placing in HNO with concentration of 20 wt.%3Soaking in the solution for 20min, washing with distilled water until the washing solution is neutral, and air drying to obtain a pretreated graphite plate;
(2) placing the graphite plate pretreated in the step (1) in the solution A, stirring and reacting for 20min at the temperature of 80 ℃ and the pH value of 11, washing with deionized water to obtain the solution containing Ag-Co3O4An activated graphite matrix of the activation layer; wherein the solution A contains 1g/L AgNO310g/L of Na2CO320mL/L hydrazine hydrate and 3g/L nano Co3O4;
(3) Coating a stainless steel wire mesh transition layer on the surface of the activated graphite substrate in the step (2), fixing the stainless steel wire mesh by using a stainless steel rivet, then placing the stainless steel wire mesh in an HC1 solution with the concentration of 10 wt.% for reaction for 2min, and washing the stainless steel wire mesh with deionized water to obtain an activated graphite substrate/stainless steel wire mesh bottom layer;
(4) placing the activated graphite substrate/stainless steel wire mesh bottom layer obtained in the step (3) in an alkaline lead acetate solution, performing electrodeposition for 3 hours at the temperature of 40 ℃ by taking a stainless steel plate as a cathode, and washing with deionized water to obtain the activated graphite substrate/stainless steel wire mesh bottom layer/composite alpha-PbO2An intermediate layer; wherein the alkaline lead acetate solution contains lead acetate (Pb (CH)3COO)2)80g/L, NaOH 200g/L and nano titanium nitride particles 10g/L, and the anode current density of electrodeposition is 2A/dm2;
(5) Activating the graphite substrate/stainless steel wire mesh bottom layer/composite alpha-PbO in the step (4)2The intermediate layer is placed in an acidic lead nitrate solution, a stainless steel pore plate is used as a cathode, electrodeposition is carried out for 8 hours at the temperature of 80 ℃, and deionized water is adopted for washing to obtain a gradient composite lead dioxide anode plate; it is composed ofThe medium-acid lead nitrate solution contains lead nitrate (Pb (NO)3)2)200g/L、HNO350g/L nano molybdenum trioxide (MoO)3) Particles 30g/L and silver nitrate (AgNO)3)50g/L, anode current density of electrodeposition is 6A/dm2;
In the acid copper electrolyte, the gradient composite lead dioxide anode plate of the embodiment has the following electrolysis conditions: the concentration of copper ions in the electrolyte is 45g/L, the concentration of sulfuric acid is 200g/L, 10mg/L of sodium fluoride and 400mg/L C1-ions are added, the electrolysis temperature is 60 ℃, and the current density is 300A/dm2Compared with the traditional lead-calcium (0.06%) tin (1.0%) alloy anode plate, the electrical efficiency of the gradient composite lead dioxide anode is improved by 3%, the cell voltage is low by 240mV, and the service life is prolonged by 2.5 times.
While the present invention has been described in detail with reference to the embodiments shown in the drawings, the present invention is not limited to the embodiments, and various changes can be made without departing from the spirit and scope of the present invention.
Claims (10)
1. A gradient composite lead dioxide anode plate is characterized in that: comprises an activated graphite matrix, a stainless steel wire mesh transition layer and a composite alpha-PbO in sequence from inside to outside2Intermediate layer and composite beta-PbO2The graphite substrate comprises flaky graphite powder, modified asphalt, copper oxide, ferrous oxide, nickel oxide and molybdenum oxide, and is compounded with alpha-PbO2The intermediate layer is alpha-PbO2-nano titanium nitride, composite beta-PbO2The active layer is silver-doped beta-PbO2-nano molybdenum trioxide.
2. The gradient composite lead dioxide anode plate of claim 1, wherein: the graphite substrate comprises, by mass, 100% of a graphite substrate, 10-18% of modified asphalt, 0.01-0.2% of copper oxide, 0.01-0.1% of ferrous oxide, 0.01-0.05% of nickel oxide, 0.01-0.05% of molybdenum oxide and the balance of flaky graphite powder.
3. The gradient composite lead dioxide anode plate of claim 1 or 2, which is characterized in thatCharacterized in that: the surface of the graphite substrate contains Ag-Co3O4Active layer of Co3O4Is nanoparticle with particle size of 10-100nm, and Ag-Co3O4The mass content of Ag in the activation layer is 20-50%.
4. The gradient composite lead dioxide anode plate of claim 1, wherein: alpha-PbO2-the thickness of the nano titanium nitride is 0.05-0.5 mm, the content of titanium nitride particles is 0.1-5 wt.%, and the particle size of the nano titanium nitride is 20-60 nm.
5. The gradient composite lead dioxide anode plate of claim 1, wherein: silver doped beta-PbO2-the thickness of the nano molybdenum trioxide is 0.1-1.5 mm, the content of molybdenum trioxide particles is 0.1-0.5 wt.%, the particle size of the nano molybdenum trioxide is 80-200nm, and the content of silver is 0.01-0.15 wt.%.
6. The preparation method of the gradient composite lead dioxide anode plate of any one of claims 1 to 5 is characterized by comprising the following specific steps:
(1) placing a graphite plate in NaOH solution, soaking for 0.5-1 h at the temperature of 60-80 ℃, cleaning with distilled water until the cleaning solution is neutral, and then placing in HNO3Soaking in the solution for 10-20 min, cleaning with distilled water until the cleaning solution is neutral, and airing to obtain a pretreated graphite plate;
(2) placing the graphite plate pretreated in the step (1) in the solution A, reacting for 2-20 min at the pH value of 9-11 and the temperature of 40-80 ℃, and washing with deionized water to obtain the solution containing Ag-Co3O4An activated graphite matrix of the activation layer; wherein solution A contains AgNO3、Na2CO3Hydrazine hydrate and nano Co3O4;
(3) Coating the surface of the activated graphite substrate in the step (2) with a stainless steel wire mesh transition layer, then placing the activated graphite substrate in HC1 solution for reaction for 0.5-2 min, and washing with deionized water until the washing solution is neutral to obtain an activated graphite substrate/stainless steel wire mesh bottom layer;
(4) activating the stone in the step (3)Placing the ink matrix/stainless steel wire mesh bottom layer in an alkaline lead acetate solution, taking a stainless steel plate as a cathode, performing electrodeposition for 1-3 h at the temperature of 40-60 ℃, and washing with deionized water to obtain the activated graphite matrix/stainless steel wire mesh bottom layer/composite alpha-PbO2An intermediate layer; wherein the alkaline lead acetate solution contains lead acetate, NaOH and nano titanium nitride particles;
(5) activating the graphite substrate/stainless steel wire mesh bottom layer/composite alpha-PbO in the step (4)2The middle layer is placed in an acidic lead nitrate solution, a stainless steel pore plate is used as a cathode, electrodeposition is carried out for 2-8 hours at the temperature of 40-80 ℃, and deionized water is adopted for washing to obtain a gradient composite lead dioxide anode plate; wherein the acid lead nitrate solution contains lead nitrate and HNO3Nano molybdenum trioxide particles and silver nitrate.
7. The method for preparing the gradient composite lead dioxide anode plate according to claim 6, is characterized in that: AgNO in solution A in step (2)3The concentration is 1-3 g/L, Na2CO3The concentration is 5-20 g/L, the concentration of hydrazine hydrate is 2-20 mL/L, and the concentration of nano Co is3O4The concentration is 0.2-3 g/L.
8. The method for preparing the gradient composite lead dioxide anode plate according to claim 6, is characterized in that: in the step (4), the concentration of lead acetate in the alkaline lead acetate solution is 40-80 g/L, the concentration of NaOH is 140-200 g/L, the concentration of nano titanium nitride particles is 2-10 g/L, and the current density of an anode for electrodeposition is 0.2-2A/dm2。
9. The method for preparing the gradient composite lead dioxide anode plate according to claim 6, is characterized in that: the concentration of the lead nitrate in the acidic lead nitrate solution in the step (5) is 100-300 g/L, HNO3The concentration is 20-50 g/L, the concentration of the nano molybdenum trioxide particles is 10-30 g/L, the concentration of silver nitrate is 20-50 g/L, and the current density of an anode of electrodeposition is 1-6A/dm2。
10. The use of the gradient composite lead dioxide anode plate of any one of claims 1 to 5 as an anode plate in copper electrodeposition.
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